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食品污染物(4-羟基壬烯醛和农药)对人类结肠细胞的短期和长期致癌作用:遗传毒性和非基因组机制的参与

Short-Term and Long-Term Carcinogenic Effects of Food Contaminants (4-Hydroxynonenal and Pesticides) on Colorectal Human Cells: Involvement of Genotoxic and Non-Genomic Mechanisms.

作者信息

Arnaud Liana C, Gauthier Thierry, Le Naour Augustin, Hashim Saleha, Naud Nathalie, Shay Jerry W, Pierre Fabrice H, Boutet-Robinet Elisa, Huc Laurence

机构信息

Toxalim (Research Centre in Food Toxicology), University of Toulouse, INRAE, ENVT, INP-Purpan, UPS, 31027 Toulouse, France.

Southwestern Medical Center Dallas, Department of Cell Biology, The University of Texas, Dallas, TX 75390, USA.

出版信息

Cancers (Basel). 2021 Aug 27;13(17):4337. doi: 10.3390/cancers13174337.

Abstract

To investigate environmental impacts upon colorectal carcinogenesis (CRC) by diet, we assessed two western diet food contaminants: 4-hydroxynonenal (HNE), a major lipid peroxidation product neoformed during digestion, and a mixture of pesticides. We used human colonic cell lines ectopically eliciting varied genetic susceptibilities to CRC: the non-transformed human epithelial colonic cells (HCECs) and their five isogenic cell lines with the loss of (Adenomatous polyposis coli) and (Tumor protein 53) and/or ectopic expression of mutated (Kristen-ras). These cell lines have been exposed for either for a short time (2-24 h) or for a long period (3 weeks) to 1 µM HNE and/or 10 µM pesticides. After acute exposure, we did not observe any cytotoxicity or major DNA damage. However, long-term exposure to pesticides alone and in mixture with HNE induced clonogenic transformation in normal HCECs, as well as in cells representing later stages of carcinogenesis. It was associated with genotoxic and non-genomic mechanisms (cell growth, metabolic reprogramming, cell mobility and epithelial-mesenchymal transition) depending on genetic susceptibility. This study demonstrated a potential initiating and promoting effect of food contaminants on CRC after long-term exposure. It supports that these contaminants can accelerate carcinogenesis when mutations in oncogenes or tumor suppressor genes occur.

摘要

为了研究饮食对结直肠癌发生的环境影响,我们评估了两种西方饮食中的食物污染物:4-羟基壬烯醛(HNE),一种在消化过程中新生的主要脂质过氧化产物,以及一种农药混合物。我们使用了对结直肠癌具有不同遗传易感性的人结肠细胞系:未转化的人结肠上皮细胞(HCECs)及其五个同源细胞系,这些同源细胞系存在腺瘤性息肉病基因(Adenomatous polyposis coli)和肿瘤蛋白53(Tumor protein 53)缺失和/或突变型 Kirsten 大鼠肉瘤病毒癌基因(Kristen-ras)的异位表达。这些细胞系分别短期(2 - 24小时)或长期(3周)暴露于1μM的HNE和/或10μM的农药中。急性暴露后,我们未观察到任何细胞毒性或严重的DNA损伤。然而,单独长期暴露于农药以及与HNE混合暴露,会在正常HCECs以及代表癌变后期阶段的细胞中诱导克隆形成转化。这与遗传易感性相关的遗传毒性和非基因组机制(细胞生长、代谢重编程、细胞迁移和上皮-间质转化)有关。这项研究表明,长期暴露后食物污染物对结直肠癌具有潜在的启动和促进作用。它支持这样的观点,即当癌基因或肿瘤抑制基因发生突变时,这些污染物会加速癌变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f97f/8431687/431e86b340b4/cancers-13-04337-g001.jpg

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